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rs863224945

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224945(C;C)
Make rs863224945(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95637381
GeneALDH18A1
is asnp
is mentioned by
dbSNPrs863224945
ebirs863224945
HLIrs863224945
Exacrs863224945
Varsomers863224945
Maprs863224945
PheGenIrs863224945
hapmaprs863224945
1000 genomesrs863224945
hgdprs863224945
ensemblrs863224945
gopubmedrs863224945
geneviewrs863224945
scholarrs863224945
googlers863224945
pharmgkbrs863224945
gwascentralrs863224945
openSNPrs863224945
23andMers863224945
23andMe allrs863224945
SNP Nexus

SNPshotrs863224945
SNPdbers863224945
MSV3drs863224945
GWAS Ctlgrs863224945
Max Magnitude0
ClinVar
Risk rs863224945(C;C)
Alt rs863224945(C;C)
Reference rs863224945(T;T)
Significance Pathogenic
Disease Spastic paraplegia 9
Variation info
Gene ALDH18A1
CLNDBN Spastic paraplegia 9
Reversed 1
HGVS NC_000010.10:g.97397138A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000200954.2,